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1.


   
    Mixed-valence hydrated iron fluoridotitanate: synthesis, optics and calorimetry / S. V. Mel'nikova, N. M. Laptash, M. V. Gorev, E. I. Pogoreltsev // J. Phys. Chem. Solids. - 2020. - Vol. 142. - Ст. 109444, DOI 10.1016/j.jpcs.2020.109444. - Cited References: 35 . - ISSN 0022-3697
Кл.слова (ненормированные):
Crystal growth -- Fluoridotitanate -- Mixed valence -- Phase transition -- Optical properties -- Heat capacity
Аннотация: Mixed-valence hydrated fluoridotitanate with idealized formula FeTiF6·6H2O is the main product of fluoride processing of natural mineral ilmenite with hydrofluoric acid. Its single crystals were grown and optical and calorimetric experiments were carried out in the temperature range 200–350 K. Charge re-distribution, Fe2+Ti4+ to Fe3+Ti3+, in the compound studied was evident in XPS spectra. A first order ferroelastic phase transition occurs at temperatures T0↓ = 271.5 K, T0↑ = 274 ÷ 275.5 K with the symmetry change P3‾↔ P1‾. The structural transformation is accompanied by the appearance of a very weak optical anisotropy in the slice (001), a small anomaly of the heat capacity (ΔS = 1.5 J/mol K = 0.2R), and positive baric coefficients dT0/dp ≈ 30 ± 10 K/GPa.

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Держатели документа:
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Institute of Chemistry, Far Eastern Branch of RAS, Vladivostok, 690022, Russian Federation
Siberian Federal University, Krasnoyarsk, 660074, Russian Federation

Доп.точки доступа:
Mel'nikova, S. V.; Мельникова, Светлана Владимировна; Laptash, N. M.; Gorev, M. V.; Горев, Михаил Васильевич; Pogoreltsev, E. I.; Погорельцев, Евгений Ильич
}
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2.


   
    Renewable P-type zeolite for superior absorption of heavy metals: Isotherms, kinetics, and mechanism / M. Chen, S. Nong, Y. Zhao [et al.] // Sci. Total Environ. - 2020. - Vol. 726. - Ст. 138535, DOI 10.1016/j.scitotenv.2020.138535. - Cited References: 47. - This work was supported by the National Key Research and Development Program of China (Grant No. 2016YFB0901600 ); National Science Foundation of China (Grant No. 21871008 ); Science and Technology Commission of Shanghai Municipality (Grant No. 14520722000 ) and China Postdoctoral Science Foundation [Grant No. 8206300161 ]. Thank Shuying Nong for her experimental assistance . - ISSN 0048-9697
Кл.слова (ненормированные):
Uptake capacity -- High efficiency -- Drinkable level -- Regeneration
Аннотация: Zeolite is a characteristic material for removing heavy metals exhibiting by low tolerance quantities. It is particularly desirable although challenging to cultivate an unmodified and reusable zeolite for eradicating heavy metals with great capacity. Herein, we sought out and firstly synthesized the uniform octahedral zeolite Na6Al6Si10O32·12H2O for heavy metal ions trap, proven extraordinarily effective decontamination of M2+ (Pb2+, Cd2+, Cu2+, and Zn2+). The maximum capacities of Pb2+, Cd2+, Cu2+, and Zn2+ were 649, 210, 90 and 88 mg/g, and the distribution coefficients (Kd) was ~108 mL/g for Pb2+ which emphasized the superior effectiveness of Na6Al6Si10O32·12H2O contrasted with other zeolites. Rapid adsorption was observed that Pb2+ concentration (7.5 ppm) was reduced to 0.6 ppb in 2 min. The removal mechanism was ascribed to the ion exchange and hydroxyl groups thereby affording high adsorption capacity. We also investigated the heavy metal removal of zeolite 13X and 4A for comparison and concluded the determining factor affecting absorption capacity. The removal rate of Pb remained at 97% even after five regeneration recycles. The zeolite was therefore promising for practical water purification and industrialization.

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Держатели документа:
Beijing National Laboratory for Molecular Sciences and State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing, 100871, China
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
CAS Key Laboratory of Materials for Energy Conversion and State Key Laboratory of High-Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai, 200050, China

Доп.точки доступа:
Chen, M.; Nong, S.; Zhao, Y.; Riaz, M. S.; Xiao, Y.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Huang, F.
}
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3.


   
    Calorimetric, dilatometric and DTA under pressure studies of the phase transitions in elpasolite (NH4)2KZrF7 / M. V. Gorev, A. V. Kartashev, E. V. Bogdanov [et al.] // J. Fluor. Chem. - 2020. - Vol. 235. - Ст. 109523, DOI 10.1016/j.jfluchem.2020.109523. - Cited References: 45. - The reported study was funded by RFBR according to the research project No. 18-02-00269 a. X-ray and dilatometric data were obtained using the equipment of Krasnoyarsk Regional Center of Research Equipment of Federal Research Center "Krasnoyarsk Science Center SB RAS" . - ISSN 0022-1139
Кл.слова (ненормированные):
Phase transition -- Fluorides -- Heat capacity -- Entropy -- Thermal expansion -- High pressure
Аннотация: Heat capacity, thermal expansion, and sensitivity to the hydrostatic pressure of (NH4)2KZrF7 elpasolite are studied in a wide temperature range. The changes in deformation and entropy during successive phase transitions are determined: Δ(ΔV/V) = 3·10−4; ΔS = 8 J/mol K The temperatures and entropies of phase transitions turned out to be slightly sensitive to pressure changes. An analysis of the entropy of phase transformations was performed in the framework of the model of the cubic phase structure Fm-3 m. In the low temperature phase, an anomalous behavior of thermodynamic properties, which is not characteristic of phase transitions, was observed, accompanied by a significant change in the crystal lattice entropy.

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Держатели документа:
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Institute of Engineering Physics and Radioelectronics, Siberian Federal University, Krasnoyarsk, 660074, Russian Federation
Astafijev Krasnoyarsk State Pedagogical University, Krasnoyarsk, 660049, Russian Federation
Institute of Engineering Systems and Energy, Krasnoyarsk State Agrarian University, Krasnoyarsk, 660049, Russian Federation
Institute of Chemistry, Far Eastern Department of RAS, Vladivostok, 690022, Russian Federation

Доп.точки доступа:
Gorev, M. V.; Горев, Михаил Васильевич; Kartashev, A. V.; Карташев, Андрей Васильевич; Bogdanov, E. V.; Богданов, Евгений Витальевич; Flerov, I. N.; Флёров, Игорь Николаевич; Laptash, N. M.
}
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4.


   
    Structure and thermodynamic properties of the SmGaGe2O7 oxide / L. T. Denisova, M. S. Molokeev, L. A. Irtyugo [et al.] // Phys. Solid State. - 2020. - Vol. 62, Is. 2. - P. 384-387, DOI 10.1134/S1063783420020109. - Cited References: 10. - This study was carried out within the state assignment of the Ministry of Science and Higher Education of the Russian Federation to the Siberian Federal University in 2017–2019, project no. 4.8083.2017/8.9 “Formation of a Data Bank of Thermodynamic Characteristics of the Complex-Oxide Multifunctional Materials Containing Rare and Scattered Elements.” . - ISSN 1063-7834
Кл.слова (ненормированные):
samarium gallium germanate -- structure -- heat capacity
Аннотация: The SmGaGe2O7 oxide material has been obtained from initial Sm2O3, Ga2O3, and GeO2 oxides by solid-phase synthesis with annealing in air in the temperature range of 1273–1473 K. The structure of the investigated germanate (sp. gr. P21/c, a = 7.18610(9) Å, b = 6.57935(8) Å, and c = 12.7932(2) Å) has been established by X-ray diffraction and the high-temperature heat capacity has been determined by differential scanning calorimetry. Using the experimental data on Cp = f(T), the thermodynamic properties of the compound have been calculated.

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Публикация на русском языке Структура и термодинамические свойства SmGaGe2O7 [Текст] / Л. Т. Денисова, М. С. Молокеев, Л. А. Иртюго [и др.] // Физ. тверд. тела. - 2020. - Т. 62 Вып. 2. - С. 332-335

Держатели документа:
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Kirensky Institute of Physics, Krasnoyarsk Scientific Center, Siberian Branch, Russian Academy of Sciences, Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Denisova, L. T.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Irtyugo, L. A.; Beletskii, V. V.; Belousova, N. V.; Denisov, V. M.
}
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5.


   
    Heat capacity, thermal expansion and barocaloric effect in fluoride K2TaF7 / I. N. Flerov [et al.] // J. Mater. Sci. - 2019. - Vol. 54, Is. 23. - P. 14287–14295, DOI 10.1007/s10853-019-03924-8. - Cited References: 20. - The reported study was funded by RFBR according to the research Project No. 18-02-00269_a. . - ISSN 0022-2461
Кл.слова (ненормированные):
Expansion -- Fluorine compounds -- Specific heat -- Tantalum compounds -- Thermal expansion -- Barocaloric effects -- First-order phase transitions -- High sensitivity -- Low pressures -- Temperature phase -- Volume strain -- Potassium compounds
Аннотация: The heat capacity and thermal expansion of potassium heptafluorotantalate were studied. The room temperature phase P21/c is stable at least to 4 K. The strong first-order phase transition P21/c−Pnma at T0=486.2K is accompanied by giant changes in the entropy, ΔS0=22.3J(molK)−1, and volume strain, δV0/V=−3.6%. A rather high sensitivity of K2TaF7 to pressure was found, dT0/dp=−220KGPa−1. Significant extensive and intensive barocaloric effects are found at low pressure. The possibility of improving the barocaloric properties is discussed.

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Держатели документа:
Kirensky Institute of Physics, Federal Research Center KSC Siberian Branch, Russian Academy of Sciences, Krasnoyarsk, 660036, Russian Federation
Institute of Engineering Physics and Radioelectronics, Siberian Federal University, Krasnoyarsk, 660074, Russian Federation
Astafijev Krasnoyarsk State Pedagogical University, Krasnoyarsk, 660049, Russian Federation
Institute of Chemistry, Far East Branch, Russian Academy of Sciences, Vladivostok, 690022, Russian Federation

Доп.точки доступа:
Flerov, I. N.; Флёров, Игорь Николаевич; Gorev, M. V.; Горев, Михаил Васильевич; Kartashev, A. V.; Карташев, Андрей Васильевич; Pogorel'tsev, E. I.; Погорельцев, Евгений Ильич; Laptash, N. M.
}
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6.


   
    Проявление спиновых корреляций в монокристалле ErAl3(BO3)4 / В. А. Бедарев [и др.] // Физ. низких температур. - 2019. - Т. 45, № 9. - С. 1217-1222. - Библиогр.: 15 . - ISSN 0132-6414. - ISSN 1816-0328
Кл.слова (ненормированные):
электронный парамагнитный резонанс -- теплоемкость -- спин-спиновое взаимодействие -- магнитные кластеры -- електронний парамагнітний резонанс -- теплоємність -- спін-спінова взаємодія -- магнітні кластери -- еlectronic paramagnetic resonance -- heat capacity -- spin-spin interaction -- magnetic clusters
Аннотация: Установлено наличие существенного магнитного вклада в удельную теплоемкость монокристалла ErAl3(BO3)4 при температурах менее 5 К. Результаты измерений спектров ЭПР при 4,2 К также свидетельствуют о проявлении ближнего магнитного порядка. Полученные данные обсуждаются в рамках модели, учитывающей спин-спиновое взаимодействие между редкоземельными ионами в парных кластерах.
Встановлено присутність суттєвого магнітного внеску в питому теплоємність монокристалу ErAl3(BO3)4 при температурах нижче 5 К. Результати вимірювань спектрів ЕПР при температурі 4,2 К також свідчать про прояв близького магнітного порядку. Отримані дані обговорюються у рамках моделі, яка враховує спін-спінову взаємодію між рідкісноземельними іонами у парних кластерах.

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Переводная версия Manifestation of Spin Correlations in Monocrystalline ErAl3(BO3)4 [Текст] / V. A. Bedarev [et al.] // Low Temp. Phys. - 2019. - Vol. 45 Is. 9.- P.1041-1045

Держатели документа:
Физико-технический институт низких температур им. Б.И. Веркина НАН Украины пр. Науки, 47, г. Харьков, 61103, Украина
Institute of Physics, Polish Academy of Sciences, Warsaw, Poland
Институт физики им. Л.В. Киренского ФИЦ КНЦ СO РАН, г. Красноярск, Россия

Доп.точки доступа:
Бедарев, В. А.; Меренков, Д. Н.; Кобец, М. И.; Звягин, А. А.; Попережай, С. Н.; Гнатченко, С. Л.; Zajarniuk, T.; Vasevych, T.; Gutowska, M. U.; Szewczyk, A.; Гудим, Ирина Анатольевна; Gudim, I. A.
}
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7.


   
    Heat capacity, structural and magnetic properties of mixed-valence Pb3(Mn,Cu)7O15 / N. V. Mikhashenok [et al.] // Euro-asian symposium "Trends in magnetism" (EASTMAG-2019) : Book of abstracts / чл. конс. ком.: S. G. Ovchinnikov, N. V. Volkov [et al.] ; чл. прогр. ком. D. M. Dzebisashvili [et al.]. - 2019. - Vol. 1. - Ст. G.03. - P. 555. - Cited References: 2 . - ISBN 978-5-9500855-7-4

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Держатели документа:
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, Russia
Institute of Chemistry and Chemical Technology, Federal Research Center KSC SB RAS, Krasnoyarsk, Russia

Доп.точки доступа:
Ovchinnikov, S. G. \чл. конс. ком.\; Овчинников, Сергей Геннадьевич; Volkov, N. V. \чл. конс. ком.\; Волков, Никита Валентинович; Dzebisashvili, D. M. \чл. прогр. ком.\; Дзебисашвили, Дмитрий Михайлович; Mikhashenok, N. V.; Михашенок, Наталья Владимировна; Soloviev, L. A.; Соловьев, Леонид Александрович; Nazarenko, I. I.; Назаренко, Илья Иванович; Eremin, E. V.; Еремин, Евгений Владимирович; Sofronova, S. N.; Софронова, Светлана Николаевна; Российская академия наук; Уральское отделение РАН; Институт физики металлов им. М. Н. Михеева Уральского отделения РАН; Уральский федеральный университет им. первого Президента России Б.Н. Ельцина; Российский фонд фундаментальных исследований; Euro-Asian Symposium "Trends in MAGnetism"(7 ; 2019 ; Sept. ; 8-13 ; Ekaterinburg); "Trends in MAGnetism", Euro-Asian Symposium(7 ; 2019 ; Sept. ; 8-13 ; Ekaterinburg)
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}
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8.


   
    Phase transition in RbCdZrF7: Structure and thermal properties / E. V. Bogdanov, M. S. Molokeev, M. V. Gorev [et al.] // J. Fluor. Chem. - 2021. - Vol. 245. - Ст. 109748, DOI 10.1016/j.jfluchem.2021.109748. - Cited References: 30. - The reported study was funded by RFBR according to the research project No. 18-02-00269 a. X-ray and dilatometric data were obtained using the equipment of Krasnoyarsk Regional Center of Research Equipment of Federal Research Center "Krasnoyarsk Science Center SB RAS" . - ISSN 0022-1139
   Перевод заглавия: Фазовый переход в RbCdZrF7: структура и термические свойства
Кл.слова (ненормированные):
Phase transition -- Fluorides -- Structure -- Heat capacity -- Entropy -- Thermal expansion
Аннотация: X-ray, calorimetric and dilatometric studies of RbCdZrF7 revealed the existence of the second order phase transition Cmcm - P21/m at T0 = 200 K. The structure of the initial and distorted phases is ordered. The phase transition is associated with displacements of fluorine atoms, which leads to minor rotations of the CdF7 and ZrF7 pentagonal bipyramids. A small change in entropy, 0.1R, is characteristic of displacive-type transformations. An anomalously high susceptibility of the transition temperature to hydrostatic pressure was found.

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Держатели документа:
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Institute of Engineering Systems and Energy, Krasnoyarsk State Agrarian University, Krasnoyarsk, 660049, Russian Federation
Institute of Engineering Physics and Radioelectronics, Siberian Federal University, Krasnoyarsk, 660074, Russian Federation
Institute of Chemistry, Far Eastern Branch of RAS, Vladivostok, 690022, Russian Federation

Доп.точки доступа:
Bogdanov, E. V.; Богданов, Евгений Витальевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Gorev, M. V.; Горев, Михаил Васильевич; Kartashev, A. V.; Карташев, Андрей Васильевич; Laptash, N. M.; Flerov, I. N.; Флёров, Игорь Николаевич
}
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9.


   
    Obtaining particles with the structure Mg@C and (Mg@C)@Pd, their properties and stability in the hydrogenation/dehydrogenation processes / G. N. Churilov, N. S. Nikolaev, V. I. Elesina [et al.] // Int. J. Hydrogen Energy. - 2022. - Vol. 47. Is. 11. - P. 7299-7309, DOI 10.1016/j.ijhydene.2021.03.042. - Cited References: 46 . - ISSN 0360-3199
   Перевод заглавия: Получение частиц со структурой Mg@C и (Mg@C)@Pd, их свойства и стабильность в процессах гидрирования /дегидрирования
Кл.слова (ненормированные):
Core-shell particles -- Mg, С, Рd nanoparticles -- Sorption capacity of hydrogen -- Hydrogen-storage materials -- Magnesium hydride
Аннотация: In this work, we studied the change in the properties of powders with a core (magnesium) – shell structure (carbon and carbon/palladium) in the process of hydrogenation/dehydrogenation with hydrogen (99.995 wt%). Magnesium powders were obtained by plasma chemical synthesis in an atmosphere of argon containing a small amount of hydrogen (2–3 at.%) and nitrogen (8–9 at.%), when performing a low-frequency arc discharge between a tungsten electrode and a magnesium melt. The shell (carbon and carbon/palladium) was deposited in a plasma generator with vortex and magnetic stabilization. For all samples, a decrease in the sorption capacity of hydrogen was observed as a result of successive cycles of sorption and desorption reactions. It was found that the reason for this fall is associated with the formation of the MgO and Mg(OH)2 phase, which prevents the diffusion of hydrogen. The carbon shell provides a more complete hydrogenation of the magnesium particles, and an additional palladium shell increases the resistance to cyclic hydrogenation/dehydrogenation and reduces the temperature of these processes. According to the data obtained, powders with particles (Mg@C)@Pd can absorb the largest amount of hydrogen (6.9 wt%) for the duration of 5 cycles, after which the protective shell of the particles begins to collapse and a loss of sorption capacity is observed.

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Держатели документа:
Institute of Engineering Physics and Radio Electronics, Siberian Federal University, Svobodny, 79, Krasnoyarsk, 660041, Russian Federation
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Akademgorodok 50/38, Krasnoyarsk, 660036, Russian Federation
Institute of Chemistry and Chemical Technology, Federal Research Center KSC SB RAS, Akademgorodok 50/24, Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Churilov, G. N.; Чурилов, Григорий Николаевич; Nikolaev, N. S.; Николаев, Никита Сергеевич; Elesina, V. I.; Елесина, Виктория Игоревна; Glushenko, G. A.; Глущенко, Гарий Анатольевич; Isakova, V. G.; Исакова, Виктория Гавриловна; Tomashevich, Y. V.
}
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10.


   
    Crystal structure and thermodynamic properties of titanate ErGaTi2O7 / L. T. Denisova, M. S. Molokeev, V. V. Ryabov [et al.] // Russ. J. Inorg. Chem. - 2021. - Vol. 66, Is. 4. - P. 532-537, DOI 10.1134/S0036023621040082. - Cited References: 29 . - ISSN 0036-0236
Кл.слова (ненормированные):
erbium gallium titanate -- solid-state synthesis -- crystal structure -- high-temperature heat capacity -- thermodynamic functions
Аннотация: Erbium gallium titanate was prepared by solid-phase synthesis via the sequential calcination of precursor oxides in an air atmosphere at 1273 and 1573 K. The crystal structure of ErGaTi2O7 was characterized by full-profile analysis for the X-ray diffraction pattern of the synthesized powder sample as follows: space group Pcnb, a = 9.77326(15) Å, b = 13.5170(2) Å, c = 7.33189(11) Å, V = 918.58(3) Å3, ρ = 6.10 g/cm3. The high-temperature heat capacity of erbium gallium titanate was measured by differential scanning calorimetry within a temperature range of 320–1000 K. Based on these data, the basic thermodynamic functions of ErGaTi2O7 were calculated.

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Публикация на русском языке Кристаллическая структура и термодинамические свойства титаната ErGaTi2O7 [Текст] / Л. Т. Денисова, М. С. Молокеев, В. В. Рябов [и др.] // Журн. неорг. химии. - 2021. - Т. 66 № 4. - С. 492-497

Держатели документа:
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Kirenskii Institute of Physics, Federal Research Center “Krasnoyarsk Scientific Center”, Siberian Branch, Russian Academy of Sciences, Krasnoyarsk, 660036, Russian Federation
Institute of Metallurgy, Ural Branch, Russian Academy of Sciences, Yekaterinburg, 620016, Russian Federation
Baikov Institute of Metallurgy and Material Science, Russian Academy of Sciences, Moscow, 119991, Russian Federation

Доп.точки доступа:
Denisova, L. T.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Ryabov, V. V.; Kargin, Y. F.; Chumilina, L. G.; Denisov, V. M.
}
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